# FDA Inspection 837222 - Elos Medtech Timmersdala AB - May 29, 2013

Source: https://www.keypedia.com/records/fda_inspections/elos-medtech-timmersdala-ab/79c650d4-12de-473c-8252-0807cfb11f34
Source feed: FDA_Inspections

> FDA Inspection 837222 for Elos Medtech Timmersdala AB on May 29, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 837222
- Company Name: Elos Medtech Timmersdala AB
- Inspection Date: 2013-05-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/elos-medtech-timmersdala-ab/0fc59f5a-6d36-43d8-b3ab-834fcaffaf36

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7